Canonical Allele Identifier: CA1729173626

Gene: CYP3A5 ZSCAN25

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99665265C= , CM000669.2:g.99665265C=	GRCh38
NC_000007.13:g.99262888C= , CM000669.1:g.99262888C=	GRCh37
NC_000007.12:g.99100824C=	NCBI36
NG_007938.1:g.19734G=
NG_007938.2:g.19734G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646887.1:c.*256G= (CYP3A5)	ENSP00000496704.1:n.*256G=
ENST00000222982.8:c.571G= (CYP3A5) MANE Select	ENSP00000222982.4:p.Val191=
ENST00000339843.6:c.*970G= (CYP3A5)	ENSP00000343074.2:n.*970G=
ENST00000461920.5:n.1163G= (CYP3A5)
ENST00000463364.5:n.890G= (CYP3A5)
ENST00000466061.5:n.911G= (CYP3A5)
ENST00000469887.5:n.1019G= (CYP3A5)
ENST00000481825.5:n.1171G= (CYP3A5)
NM_000777.4:c.571G= (CYP3A5)	NP_000768.1:p.Val191=
NM_001291829.1:c.232G= (CYP3A5)	NP_001278758.1:p.Val78=
NM_001291830.1:c.541G= (CYP3A5)	NP_001278759.1:p.Val181=
NR_033807.2:n.1220G= (CYP3A5)
XM_006715859.2:c.571G= (CYP3A5)	XP_006715922.1:p.Val191=
XM_011515843.1:c.232G= (CYP3A5)	XP_011514145.1:p.Val78=
XM_011515844.1:c.232G= (CYP3A5)	XP_011514146.1:p.Val78=
XM_011515845.1:c.31G= (CYP3A5)	XP_011514147.1:p.Val11=
XM_011515846.1:c.31G= (CYP3A5)	XP_011514148.1:p.Val11=
XM_011515847.1:c.31G= (CYP3A5)	XP_011514149.1:p.Val11=
XM_011515909.1:c.806-3830C= (ZSCAN25)	XP_011514211.1:n.806-3830C=
XR_927402.1:n.1466+41085C= (ZSCAN25)
NM_000777.5:c.571G= (CYP3A5) MANE Select	NP_000768.1:p.Val191=
NM_001350984.1:c.806-3830C= (ZSCAN25)	NP_001337913.1:n.806-3830C=
NM_001350985.1:c.806-3830C= (ZSCAN25)	NP_001337914.1:n.806-3830C=
XM_011515909.2:c.806-3830C= (ZSCAN25)	XP_011514211.1:n.806-3830C=
XR_927402.2:n.1465+41085C= (ZSCAN25)
NM_001291829.2:c.232G= (CYP3A5)	NP_001278758.1:p.Val78=
NM_001291830.2:c.541G= (CYP3A5)	NP_001278759.1:p.Val181=
NM_001350984.2:c.806-3830C= (ZSCAN25)	NP_001337913.1:n.806-3830C=
NM_001350985.2:c.806-3830C= (ZSCAN25)	NP_001337914.1:n.806-3830C=
NR_033807.3:n.1190G= (CYP3A5)